Evidence map›Paper›PMID 41860697›Full record

ArticleClinical rheumatology2026

CD161⁺ Treg as a potential biomarker for evaluating disease activity and treatment efficacy in rheumatoid arthritis.

Ziyi Song, Danxue Zhu, Feng Sun, Jiayi Geng, Chuanhui Xu, Junyi Jiang, Wenjuan Zhang, Xiaolin Sun, Zhanguo Li

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Article in Clinical rheumatology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
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1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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3 · Its place in the literature

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1 citing paper in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

9 authors.

Ziyi Song *Department of Rheumatology and Immunology, Peking University People's Hospital, Beijing, 100044, China.
Danxue Zhu *Department of Rheumatology and Immunology, Peking University People's Hospital, Beijing, 100044, China.
Feng SunDepartment of Rheumatology and Immunology, Peking University People's Hospital, Beijing, 100044, China.
Jiayi GengDepartment of Thoracic Surgery, Peking University People's Hospital, Beijing, 100044, China.
Chuanhui XuDepartment of Rheumatology, Allergy and Immunology, Tan Tock Seng Hospital, Jln Tan Tock Seng, Singapore, 308433, Singapore.
Junyi JiangState Key Laboratory of Medical Proteomics, Beijing Proteome Research Center, National Center for Protein Sciences (Beijing), Beijing Institute of Lifeomics, Beijing, China.
Wenjuan ZhangState Key Laboratory of Medical Proteomics, Beijing Proteome Research Center, National Center for Protein Sciences (Beijing), Beijing Institute of Lifeomics, Beijing, China.
Xiaolin SunDepartment of Rheumatology and Immunology, Peking University People's Hospital, Beijing, 100044, China. sunxiaolin_sxl@126.com.ORCID http://orcid.org/0000-0001-9709-1532
Zhanguo LiDepartment of Rheumatology and Immunology, Peking University People's Hospital, Beijing, 100044, China. li99@bjmu.edu.cn.

Funding

National Natural Science Foundation of China 32141004National Natural Science Foundation of China 82171775National Natural Science Foundation of China 82230119National Natural Science Foundation of China 92374202
6 · The paper itself

Abstract

backgroundCD161⁺ regulatory T cells (Tregs) are involved in rheumatoid arthritis (RA) pathogenesis. This study aimed to investigate the levels of circulating CD161⁺ Tregs in RA patients and to evaluate their associations with clinical features, laboratory indicators, and therapeutic responses.

methodsA total of 172 RA patients meeting the 2010 ACR/EULAR criteria and 110 age- and sex-matched healthy controls (HCs) were enrolled. The proportion of CD161⁺ Tregs in peripheral blood was quantified by flow cytometry. Correlations between CD161⁺ Treg levels and clinical manifestations, laboratory parameters, and disease activity scores (DAS28) were assessed. Twenty-four RA patients were longitudinally followed to assess post-treatment changes in CD161⁺ Tregs and disease activity.

resultsThe proportions of CD161⁺ Tregs of the total Treg and CD4⁺ T cell populations were significantly elevated in RA patients compared to HCs (P < 0.001). Higher CD161⁺ Treg levels were associated with smoking history (P = 0.033) and inversely correlated with the presence of dry eye sicca (P = 0.030). These subsets showed positive correlations with IgA, IgM, rheumatoid factor (RF), RF-IgG, TNF-α

conclusionCD161⁺ Tregs are elevated in RA and associated with disease activity and immunologic indicators. CD161⁺ Tregs might serve as a biomarker for assessing RA disease activity. Key Points • The proportion of circulating CD161⁺ regulatory T cells is significantly increased in rheumatoid arthritis patients compared to healthy controls. • Higher CD161⁺ Treg levels correlate positively with disease activity scores (DAS28-ESR) and key serological markers (RF, IgA, IgM). • CD161⁺ Treg levels decreased significantly following effective therapy, paralleling reductions in disease activity, particularly in the group receiving csDMARDs combined with tocilizumab. • CD161⁺ Tregs show positive correlations with pro-inflammatory cells (TNF-α+CD4+T cell, Th17) and peripheral T follicular helper cells, underscoring their role in RA immunopathology.

Indexed as

Arthritis, RheumatoidNK Cell Lectin-Like Receptor Subfamily BT-Lymphocytes, RegulatoryAdultAgedAntirheumatic AgentsBiomarkersCase-Control StudiesDisease ProgressionFemaleFlow CytometryHumansLongitudinal StudiesMaleMiddle AgedSeverity of Illness IndexAntirheumatic AgentsBiomarkersKLRB1 protein, humanNK Cell Lectin-Like Receptor Subfamily BBiomarkerCD161⁺ TregsDisease activityRheumatoid arthritisTherapeutic response

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.